Hayashi Y - Search Results

1

Mutation and expression analyses of the MET and CDKN2A genes in rhabdomyosarcoma with emphasis on MET overexpression.

Chen Y, Takita J, Mizuguchi M, Tanaka K, Ida K, Koh K, Igarashi T, Hanada R, Tanaka Y, Park MJ, Hayashi Y. Chen Y, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2007 Apr;46(4):348-58. doi: 10.1002/gcc.20416. Genes Chromosomes Cancer. 2007. PMID: 17243166

2

SEPTIN6, a human homologue to mouse Septin6, is fused to MLL in infant acute myeloid leukemia with complex chromosomal abnormalities involving 11q23 and Xq24.

Ono R, Taki T, Taketani T, Kawaguchi H, Taniwaki M, Okamura T, Kawa K, Hanada R, Kobayashi M, Hayashi Y. Ono R, et al. Among authors: hayashi y. Cancer Res. 2002 Jan 15;62(2):333-7. Cancer Res. 2002. PMID: 11809673

3

Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors.

Uno K, Takita J, Yokomori K, Tanaka Y, Ohta S, Shimada H, Gilles FH, Sugita K, Abe S, Sako M, Hashizume K, Hayashi Y. Uno K, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2002 May;34(1):33-41. doi: 10.1002/gcc.10052. Genes Chromosomes Cancer. 2002. PMID: 11921280

4

The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9.

Taketani T, Taki T, Ono R, Kobayashi Y, Ida K, Hayashi Y. Taketani T, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2002 Aug;34(4):437-43. doi: 10.1002/gcc.10077. Genes Chromosomes Cancer. 2002. PMID: 12112533

5

Lack of aberrations of the BMP4, BMP2, and PTX1 genes in a patient with pituitary hypoplasia, os odontoideum, renal dysplasia, and right leg anomalies.

Goto M, Takita J, Hashimoto N, Tateshita F, Toyoji H, Kato H, Egi S, Hayashi Y. Goto M, et al. Among authors: hayashi y. Int J Mol Med. 2002 Sep;10(3):293-7. Int J Mol Med. 2002. PMID: 12165803

6

Novel NUP98-HOXC11 fusion gene resulted from a chromosomal break within exon 1 of HOXC11 in acute myeloid leukemia with t(11;12)(p15;q13).

Taketani T, Taki T, Shibuya N, Kikuchi A, Hanada R, Hayashi Y. Taketani T, et al. Among authors: hayashi y. Cancer Res. 2002 Aug 15;62(16):4571-4. Cancer Res. 2002. PMID: 12183408

7

The kinesin superfamily protein Rab6KIFL is not involved in the pathophysiology of Charcot-Marie-Tooth disease type 4C.

Nagura M, Nagao Y, Takita J, Igarashi T, LeGuern E, Hayashi Y. Nagura M, et al. Among authors: hayashi y. Int J Mol Med. 2003 Jan;11(1):45-7. Int J Mol Med. 2003. PMID: 12469216

8

A family of episodic ataxia type 2: no evidence of genetic linkage to the CACNA1A gene.

Hirose H, Arayama T, Takita J, Igarashi T, Hayashi Y, Nagao Y. Hirose H, et al. Among authors: hayashi y. Int J Mol Med. 2003 Feb;11(2):187-9. Int J Mol Med. 2003. PMID: 12525875

9

Breakpoints at 1p36.3 in three MDS/AML(M4) patients with t(1;3)(p36;q21) occur in the first intron and in the 5' region of MEL1.

Xinh PT, Tri NK, Nagao H, Nakazato H, Taketazu F, Fujisawa S, Yagasaki F, Chen YZ, Hayashi Y, Toyoda A, Hattori M, Sakaki Y, Tokunaga K, Sato Y. Xinh PT, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2003 Mar;36(3):313-6. doi: 10.1002/gcc.10176. Genes Chromosomes Cancer. 2003. PMID: 12557231

10

Fusion of an AF4-related gene, LAF4, to MLL in childhood acute lymphoblastic leukemia with t(2;11)(q11;q23).

Hiwatari M, Taki T, Taketani T, Taniwaki M, Sugita K, Okuya M, Eguchi M, Ida K, Hayashi Y. Hiwatari M, et al. Among authors: hayashi y. Oncogene. 2003 May 8;22(18):2851-5. doi: 10.1038/sj.onc.1206389. Oncogene. 2003. PMID: 12743608

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